Colobome palpébral supérieur congénital et familial : L'opthalmologie pédiatrique = Familial and congenital upper eyelid colobomaNEZZAR, H; SYLLA, F; DALENS, H et al.Images en ophtalmologie. 2012, Vol 6, Num 3, pp 84-87, issn 1961-3172, 4 p.Article

Case of chromosome 6p25 terminal deletion associated with axenfeld-rieger syndrome and persistent hyperplastic primary vitreousSUZUKI, Katsuhiro; NAKAMURA, Makoto; AMANO, Emi et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 5, pp 503-508, issn 1552-4825, 6 p.Article

The role of midface lift and lateral canthal repositioning in the management of euryblepharonYIP, Chee-Chew; MCCANN, John D; GOLDBERG, Robert A et al.Archives of ophthalmology (1960). 2004, Vol 122, Num 7, pp 1075-1077, issn 0003-9950, 3 p.Article

Listing's law: Clinical significance and implications for neural controlWONG, Agnes M. F.Survey of ophthalmology. 2004, Vol 49, Num 6, pp 563-575, issn 0039-6257, 13 p.Article

Congenital double crystalline lensesTHAKKAR, Hansa H; SINGH, Raminder.Journal of cataract and refractive surgery. 2003, Vol 29, Num 2, pp 405-406, issn 0886-3350, 2 p.Article

Bilateral congenital trigemino-abducens synkinesisLAI, Tze; CHEN, Celia; SELVA, Dinesh et al.Archives of ophthalmology (1960). 2003, Vol 121, Num 12, pp 1796-1797, issn 0003-9950, 2 p.Article

Three novel PAX6 mutations in patients with aniridiaZUMKELLER, W; ORTH, U; GAL, A et al.MP. Molecular pathology. 2003, Vol 56, Num 3, pp 180-183, issn 1366-8714, 4 p.Article

Combination of diaphragmatic eventration and microphthalmia/anophthalmia is probably nonrandomSTEINER, Robert D; DIGNAN, Peter St. J; HOPKIN, Robert J et al.American journal of medical genetics. 2002, Vol 108, Num 1, pp 45-50, issn 0148-7299Article

Dislocation of lenses in Seckel syndromeSEIDER, Nir; BEIRAN, Itzchak; GELFAND, Yuval et al.Journal of pediatric ophthalmology and strabismus. 2002, Vol 39, Num 4, pp 237-238, issn 0191-3913Article

Fraser syndrome and cryptophthalmos: review of the diagnostic criteria and evidence for phenotypic modules in complex malformation syndromesSLAVOTINEK, A. M; TIFFT, C. J.Journal of medical genetics. 2002, Vol 39, Num 9, pp 623-633, issn 0022-2593Article

Prediction by FISH analysis of the occurrence of Wilms tumor in aniridia patientsMUTO, Reiko; YAMAMORI, Shunji; OHASHI, Hirofumi et al.American journal of medical genetics. 2002, Vol 108, Num 4, pp 285-289, issn 0148-7299Article

The complexities of ocular geneticsSALEEM, R. A; WALTER, M. A.Clinical genetics. 2002, Vol 61, Num 2, pp 79-88, issn 0009-9163Article

Amaurose congénitale de Leber de type colobome maculaire : A propos de trois cas familiaux = Macular coloboma type Leber's congenital amaurosisKIRATLI, H; BOZKURT, B.Journal français d'ophtalmologie. 2002, Vol 25, Num 1, pp 67-70, issn 0181-5512Article

CHARGE association in a 19-year-old womanENDO, Machi; HAYASAKA, Seiji; YANAGISAWA, Shuichiro et al.Annals of ophthalmology. 2002, Vol 34, Num 4, pp 234-237, issn 1530-4086, 4 p.Article

Computed tomography of a cyclotocephalic neonateLOURYAN, S; VANMUYLDER, N; ROOZE, M et al.Surgical and radiologic anatomy (Print). 2002, Vol 24, Num 5, pp 319-323, issn 0930-1038, 5 p.Article

Diffuse hyperplasia of intratarsal ectopic lacrimal gland tissueLEE, William R; AITKEN, Dorothy A; KIRKNESS, Colin M et al.Archives of ophthalmology (1960). 2002, Vol 120, Num 12, pp 1748-1752, issn 0003-9950, 5 p.Conference Paper

A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eyeNISHIMURA, Darryl Y; SEARBY, Charles C; SHEFFIELD, Val C et al.American journal of human genetics. 2001, Vol 68, Num 2, pp 364-372, issn 0002-9297Article

Arrhythmicity in a child with septo-optic dysplasia and establishment of sleep-wake cyclicity with melatoninRIVKEES, Scott A.The Journal of pediatrics. 2001, Vol 139, Num 3, pp 463-465, issn 0022-3476Article

Exclusion of SIX6 hemizygosity in a child with anophthalmia, panhypopituitarism and renal failureRAUCHMAN, Michael; HOFFMAN, William H; HANNA, James D et al.American journal of medical genetics. 2001, Vol 104, Num 1, pp 31-36, issn 0148-7299Article

Autosomal dominant microcephaly-lymphoedema-chorioretinal dysplasia syndromeCASTEELS, I; DEVRIENDT, K; LEYS, A et al.British journal of ophthalmology. 2001, Vol 85, Num 4, pp 499-500, issn 0007-1161Article

Contractile peripapillary staphyloma with light stimulus to the contralateral eyeFARAH, Michel E; UNO, Fausto; BONOMO, Pedro P et al.Archives of ophthalmology (1960). 2001, Vol 119, Num 8, pp 1216-1217, issn 0003-9950Article

Orbital cavitary rhabdomyosarcoma masquerading as lymphangiomaFETKENHOUR, Douglas R; SHIELDS, Carol L; CHAO, An N et al.Archives of ophthalmology (1960). 2001, Vol 119, Num 8, pp 1208-1210, issn 0003-9950Article

Retinoblastoma protein in microphthalmic miceRICHTER, J; BRYLLA, E; LENK, C et al.Experimental and toxicologic pathology (Print). 2000, Vol 52, Num 1, pp 17-22, issn 0940-2993Article

Microblepharon : A case reportJORDAN, David R; HWANG, Ivan P; PASHBY, Robert et al.Ophthalmic surgery and lasers. 2000, Vol 31, Num 6, pp 502-505, issn 1082-3069Article

Conduite à tenir devant une anomalie du segment postérieur chez l'enfant : Principales étiologies = Posterior segment anomalies in children: principle etiologyLESUEUR, L.Journal français d'ophtalmologie. 2000, Vol 23, Num 9, pp 917-925, issn 0181-5512Conference Paper